Muscle Diseases Flashcards

1
Q

how do muscles diseases typically present?

A

myalgia
muscle weakness
stiffness
abnormal bloods

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2
Q

name the 2 inflammatory myopathies

A

polymyositis

dermatomyositis

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3
Q

most common age to be affected by an inflammatory myopathy

A

40-50 years

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4
Q

features of inflammatory myopathies on muscle biopsy

A

muscle fibre necrosis
degeneration
regeneration
inflammatory cell infiltrate

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5
Q

is muscle weakness usually symmetrical or asymmetrical?

A

symmetrical

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6
Q

what is gottrons sign

A

symmetric, occasionally scaling, violaceous erythematous eruption over the extensor surfaces of the metacarpophalangeal and interphalangeal joints of the fingers

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7
Q

which muscle disease is associated with a heliotype rash?

A

dermatomyositis

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8
Q

GI effects of dermatomyositis

A

dysphagia

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9
Q

CV effects of dermatomyositis

A

myocarditis

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10
Q

lung effects of dermatomyositis

A

ILD

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11
Q

which muscle disease is most likely to get malignancy?

A

dermatomyositis

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12
Q

most common malignancies to arise in muscle disease

A
ovarian
breast
stomach
lung
bladder
colon
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13
Q

presenting symptoms of dermatomyositis

A
tired muscles
functional difficulty
raynauds
weight loss
cough
breathlessness
muscle pain
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14
Q

what is confrontational testing?

A

direct testing of power eg pushing arm down while they resist

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15
Q

what is isotonic testing

A

30 sec sit to stand test

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16
Q

blood tests used in polymyositis?

A

CK
inflammatory markers
electrolytes, calcium, PTH, TSH
ANA, Anti-Jo-1

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17
Q

what is CK

A

a muscle enzyme

18
Q

what is electromyography

A

increasing fibrillations, abnormal motor potentials, complex repetitive discharges

19
Q

diagnostic techniques for myositis

A

muscle biopsy
MRI
EMG

20
Q

treatment for myositis

A

glucocorticoids
azathioprine
methotrexate

21
Q

most common misdiagnosis for inclusion body myositis

A

polymyositis

22
Q

presenting feature of inclusion body myositis

A

distal muscle weakness

23
Q

why is inclusion body myositis called this?

A

inclusion bodies on biopsy

24
Q

are CK levels higher in inclusion body myositis or polymyositis

A

polymyositis

25
age group affected by polymyalgia rheumatica?
over 50s
26
which areas of the world most commonly get it
northern countries
27
what disease is polymyalgia rheumatica commonly associated with?.
temporal arteritis/giant cell arteritis
28
clinical presentation of polymyalgia rheumatica
morning stiffness that improves throughout the day ache in shoulder/hip symmetrical "cant get out of bed"
29
clinical presentation of the arteritis that follows polymyalgia rheumatica
headache scalp tenderness jaw claudication visual loss (if optic artery damaged)
30
does inclusion body myositis affect the distal muscles?
yes
31
does polymyositis affect the distal muscles
no, affects proximal
32
which inflammatory markers are raised in polymyalgia rheumatica
raised ESR, plasma viscosity, CRP
33
treatment of PMR?
very good reaction to low dose steroids | if arteritis, higher dose
34
who commonly gets fibromyalgia
women of child bearing age
35
what causes fibromyalgia
depression | stress
36
clinical presentation of fibromyalgia
``` muscle stiffness pain muscle tension fatigue trouble sleeping chest pain headache cognitive difficulty worse on exertion ```
37
what pathogenic processes occur in fibromyalgia
hypersensitivity to pain
38
associated conditions to fibromyalgia
depression | IBS
39
treatment for myalgia
antidepressants strong analgesics eg gabapentin, pregabalin, mild opiates physio/OT/cognitive behavioural therapy
40
elderly man with heavy feeling in arms struggling to climb stairs with a high CK
polymyositis